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rs397516184

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397516184(A;T)
Make rs397516184(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position23420116
GeneMYH7
is asnp
is mentioned by
dbSNPrs397516184
ebirs397516184
HLIrs397516184
Exacrs397516184
Varsomers397516184
Maprs397516184
PheGenIrs397516184
hapmaprs397516184
1000 genomesrs397516184
hgdprs397516184
ensemblrs397516184
gopubmedrs397516184
geneviewrs397516184
scholarrs397516184
googlers397516184
pharmgkbrs397516184
gwascentralrs397516184
openSNPrs397516184
23andMers397516184
23andMe allrs397516184
SNP Nexus

SNPshotrs397516184
SNPdbers397516184
MSV3drs397516184
GWAS Ctlgrs397516184
Max Magnitude0
ClinVar
Risk rs397516184(T;T)
Alt rs397516184(T;T)
Reference rs397516184(A;A)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene MYH7
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.23889325T>A
CLNSRC ClinVar
CLNACC RCV000035854.2,